ERIODICTYOL
Contact usChina cas 552-58-9 factory wholesale ERIODICTYOL at affordable price
- Molecular Formula: C15H12 O6
- Molecular Weight: 288.257
- Appearance/Colour: Needle crystalline powder
- Vapor Pressure: 3.19E-16mmHg at 25°C
- Melting Point: 270°C
- Refractive Index: 1.724
- Boiling Point: 625.2 °C at 760 mmHg
- PKA: 7.49±0.40(Predicted)
- Flash Point: 241.9 °C
- PSA: 107.22000
- Density: 1.586 g/cm3
- LogP: 2.21550
ERIODICTYOL(Cas 552-58-9) Usage
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Biochem/physiol Actions |
The flavanone eriodictyol is a metabolite in the flavonoid biosynthesis pathway. Eriodictyol has anti-inflammatory and antioxidant activities and taste-modifying properties; it is extracted from plants such as Eriodictyon californicum, the twigs of Millettia duchesnei, in Eupatorium arnottianum, lemons and as glycoside in rose hips (Rosa canina). |
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Definition |
ChEBI: A tetrahydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 7, 3' and 4' respectively. |
InChI:InChI=1/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2
552-58-9 Relevant articles
TNF-α inhibition elicited by mansoins A and B, heterotrimeric flavonoids isolated from mansoa hirsuta
Campana, Priscilla R. V.,Coleman, Christina M.,Teixeira, Mauro M.,Ferreira, Daneel,Braga, Fern?o C.
, p. 824 - 830 (2014)
Mansoins A (1) and B (2) isolated from t...
Discovery of Novel Bacterial Chalcone Isomerases by a Sequence-Structure-Function-Evolution Strategy for Enzymatic Synthesis of (S)-Flavanones
Bornscheuer, Uwe T.,Brückner, Stephan I.,Gei?ler, Torsten,Gross, Egon,Hartmann, Beate,Ley, Jakob P.,Meinert, Hannes,R?ttger, Carsten,Schuiten, Eva,Yi, Dong,Zirpel, Bastian
supporting information, p. 16874 - 16879 (2021/07/06)
Chalcone isomerase (CHI) is a key enzyme...
Optimization of the biosynthesis of b-ring ortho-hydroxy lated flavonoids using the 4-hydroxyphenylacetate 3-hydroxylase complex (Hpabc) of escherichia coli
Chen, Yang,Gao, Liping,Gui, Lin,Guo, Lina,Lei, Ting,Li, Yan,Ma, Xiubing,Ruan, Haixiang,Wang, Longji,Wang, Yunsheng,Xia, Tao
, (2021/05/31)
Flavonoids are important plant metabolit...
Convenient synthesis of flavanone derivatives via oxa-Michael addition using catalytic amount of aqueous cesium fluoride
Miura, Motofumi,Shigematsu, Karin,Toriyama, Masaharu,Motohashi, Shigeyasu
, (2021/10/25)
A total of 36 flavanones, which included...
Semi-synthesis method of eriodictyol
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Paragraph 0028; 0030-0046, (2021/05/29)
The invention relates to the field of ch...
552-58-9 Process route
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520-29-6,2957-21-3,17784-36-0,118244-13-6
(-)-(S)-sakuranetin
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93012-86-3
7-methoxy-3',4',5-trihydroxyflavanone
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552-58-9
eriodictyol
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21785-09-1
7-methoxyflavanone
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480-41-1
naringenin
| Conditions | Yield |
|---|---|
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With
cytochromes P450 in human liver microsomes;
Kinetics;
Enzymatic reaction;
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(S)-eriodictyol-7-O-(6′′-O-malonyl)-β-D-glucopyranoside
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50-99-7
D-glucose
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552-58-9
eriodictyol
| Conditions | Yield |
|---|---|
|
With
trifluoroacetic acid;
at 110 ℃;
for 2h;
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552-58-9 Upstream products
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480-18-2
taxifolin
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480-41-1
naringenin
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446-71-9
homoeriodictyol
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1573206-81-1
(2S)-6,8-di[(1S)-(2'-O-β-D-glucopyranosyl-4'-hydroxyphenyl)-3-(4-hydroxyphenyl)propyl]-3'-O-β-D-glucopyranosyleryodyctiol
552-58-9 Downstream products
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10210-16-9
tertra-O-acetyleriodictyol
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6599-89-9
5,7,3',4'-tetrahydroxyflavanone tetraacetate
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446-71-9
homoeriodictyol
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16975-93-2
4',5,7-tetrahydroxyflavylium
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